Canonical Allele Identifier: PA2826146892
Gene: PEX11B HGNC NCBI

Linked Data

ClinVar Variation Id: 2131408
ClinVar RCV Id: RCV003052436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171724.1:p.Asp203Tyr
CA342120677
NM_001184795.1:c.607G>T